Exercise ameliorates cognition impairment due to restraint stress-induced oxidative insult and reduced BDNF level

被引:58
作者
Kwon, Dong-Ho [1 ]
Kim, Bum-Soo [1 ]
Chang, Hyukki [2 ]
Kim, Young-In [3 ]
Jo, Sangmee Ahn [4 ]
Leem, Yea-Hyun [4 ]
机构
[1] Sungshin Womens Univ, Dept Sports & Leisure, Seoul 136742, South Korea
[2] Seoul Womens Univ, Dept Human Movement, Seoul 139774, South Korea
[3] Dankook Univ, Coll Sports Sci, Cheonan Si 330951, Chungnam, South Korea
[4] Dankook Univ, Coll Pharm, Dept Pharm, Cheonan Si 330951, Chungnam, South Korea
关键词
Restraint stress; Chronic exercise; Oxidative insult; BDNF; CREB; NEUROTROPHIC FACTOR BDNF; LIPID-PEROXIDATION; APICAL DENDRITES; MESSENGER-RNA; BRAIN; HIPPOCAMPUS; ATROPHY; PROTEIN; ACID; RATS;
D O I
10.1016/j.bbrc.2013.02.111
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
We assessed whether chronic treadmill exercise attenuated restraint stress-induced cognition impairment. Although serum corticosterone was not significantly altered by exercise, the restraint-induced increases in hippocampal malondialdehyde (MDA) and 4-hydroxynonenal (HNE) were reduced by chronic exercise. The exercise paradigm also reversed stress-induced reductions in brain-derived neurotrophic factor (BDNF), which increased cAMP response element-binding protein (CREB) and ART activation. We verified the relationship between oxidative stress and BDNF signaling by treating primary hippocampal cultures with hydrogen peroxide (H2O2), which reduced BDNF and phosphorylated CREB and ART (p-CREB, p-AKT) in a dose-dependent manner. Notably, pretreatment with N-acetylcysteine (NAC) reversed these decreases in a dose-dependent manner. These findings suggest that chronic exercise can ameliorate repeated stress-induced cognitive impairment by detoxifying reactive oxygen species (ROS) in the hippocampus and activating BDNF signaling. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:245 / 251
页数:7
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